Canonical Allele Identifier: CA427808011
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1684148070
MyVariant Identifiers: chr2:g.96919717T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96253979T>C , CM000664.2:g.96253979T>C GRCh38
NC_000002.11:g.96919717T>C , CM000664.1:g.96919717T>C GRCh37
NC_000002.10:g.96283444T>C NCBI36
NG_027695.1:g.17035A>G , LRG_528:g.17035A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.546A>G MANE Select ENSP00000258439.3:p.Gly182=
ENST00000258439.7:c.546A>G ENSP00000258439.2:p.Gly182=
ENST00000432959.1:c.546A>G ENSP00000416660.1:p.Gly182=
ENST00000435268.1:c.294A>G ENSP00000411810.1:p.Gly98=
NM_001193304.2:c.546A>G NP_001180233.1:p.Gly182=
NM_017849.3:c.546A>G , LRG_528t1:c.546A>G NP_060319.1:p.Gly182=
XM_017004450.1:c.-373A>G XP_016859939.1:n.-373A>G
XM_017004452.1:c.294A>G XP_016859941.1:p.Gly98=
NM_001193304.3:c.546A>G NP_001180233.1:p.Gly182=
NM_017849.4:c.546A>G MANE Select NP_060319.1:p.Gly182=